Tele-Rehabilitation Study for People With a History of Stroke

Baycrest

Status: Completed

Conditions: Stroke

Treatments: Behavioral: Cognitive Orientation to Occupational Preformance (COOP)

Study type: Interventional

Funder types: Other

Identifiers

NCT02724813

REB#15-37

Details and patient eligibility

About

Stroke results in long-term disability for many people, and particularly for survivors of stroke who have cognitive impairments. However, a decreasing proportion of stroke patients are able to access or receive publicly funded rehabilitation. The investigators have shown in previous studies that in-person delivery of the Cognitive Orientation to daily Occupational Performance (CO-OP) rehabilitation approach to promoting attainment of everyday life goals has resulted in improvements in functional independence and executive function. In a small pilot study of tele-CO-OP with people with chronic traumatic brain injury (TBI) (n=3), the investigators found the delivery method was feasible and that participants were satisfied with the treatment and demonstrated clinically significant improvements on personally meaningful activities. The investigators will investigate the feasibility, preliminary efficacy, and cost-effectiveness of delivering CO-OP in an online format to reduce disability post-stroke. The study design is a single-blind (assessor), randomized wait-list control trial with a one-month retention follow-up. All therapy and testing sessions will be delivered online. We hypothesize that participants will demonstrate improvement in everyday activities and community participation.

Enrollment: 24 estimated patients

Sex: All

Ages: 18 to 85 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Community-dwelling adults at least three months post-stroke
• Fluent in written and spoken English
• Impairment of executive cognitive functions
• Ability to self-identify specific areas of difficulty in their everyday life that they would like to improve
• Access to a computer or tablet with a high-speed internet connection

Exclusion criteria

• Presence of dementia
• Severe concurrent depression
• Severe aphasia
• Concurrent substance abuse

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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24 participants in 2 patient groups

Intervention arm

Experimental group

Description:

Participants will receive 16 one-hour tele-CO-OP sessions delivered over a 10-week period by a licensed health care professional. We will deliver tele-CO-OP via Skype™ and record all sessions using Pamela software for Skype™.

Treatment:

Behavioral: Cognitive Orientation to Occupational Preformance (COOP)

Wait-list arm

Active Comparator group

Description:

Participant in this arm will receive therapy 8 weeks after initial assessment. Participants will receive 16 one-hour tele-CO-OP sessions delivered over a 10-week period by a licensed health care professional. We will deliver tele-CO-OP via Skype™ and record all sessions using Pamela software for Skype™.

Treatment:

Behavioral: Cognitive Orientation to Occupational Preformance (COOP)